EP0986304A1 - Fungizide mischung - Google Patents
Fungizide mischungInfo
- Publication number
- EP0986304A1 EP0986304A1 EP98929343A EP98929343A EP0986304A1 EP 0986304 A1 EP0986304 A1 EP 0986304A1 EP 98929343 A EP98929343 A EP 98929343A EP 98929343 A EP98929343 A EP 98929343A EP 0986304 A1 EP0986304 A1 EP 0986304A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- iii
- triazol
- dichlorophenyl
- compound
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
Definitions
- the present invention relates to a fungicidal mixture which
- X is CH and N
- n is 0, 1 or 2
- R is halogen, C 1 -C 4 -alkyl and C 1 -C 4 -haloalkyl, where the radicals R can be different if n is 2, or
- the invention relates to methods for controlling harmful fungi with mixtures of the compounds I (I.a and I.b), II (Il.a, Il.b and II. C) and III (III.1 - III.33).
- Il.a (common name: fenpropimorph): CAS RN [67564-91-4], US-A 4,202,894;
- Il.b (common name: tridemorph): CAS RN [81412-43-3], DE-A 11 64 152;
- 111.17 (common name: ipconazole): CAS RN [125225-28-7], EP-A 267 778;
- EP-A 645 087 discloses synergistic mixtures of the compound I.b with active ingredients II.a to II.
- C and EP-A 645 091 discloses synergistic mixtures of the compound I.b with some of the active ingredients III.1 to III.33.
- the present invention was based on the problem of mixtures which were applied with a reduced total amount
- Active substances have an improved action against harmful fungi (synergistic mixtures).
- Formula I.a in particular represents carbamates in which the combination of the substituents corresponds to one row of the following table:
- the compounds Ia.12, Ia.23, Ia.32 and Ia.38 are particularly preferred. Because of the basic character of the nitrogen atoms contained in them, the compounds I, II and III are able to form salts or adducts with inorganic or organic acids or with metal ions.
- inorganic acids examples include hydrohalic acids such as hydrogen fluoride, hydrogen chloride, hydrogen bromide and hydrogen iodide, carbonic acid, sulfuric acid, phosphoric acid and nitric acid.
- organic acids are formic acid and alkanoic acids, such as acetic acid, trifluoroacetic acid, trichloroacetic acid and propionic acid, and glycolic acid, thiocyanic acid, lactic acid, succinic acid, citric acid, benzoic acid, cinnamic acid, oxalic acid, alkylsulfonic acids (sulfonic acids with straight-chain alkyl radicals or branched-chain alkyl radicals or branched-chain alkyl radicals or branched-chain alkyl radicals or branched-chain alkyl radicals or branched-chain alkyl radicals or branched-chain alkyl radicals, or branched-chain alkyl radicals or branched-chain alkyl radicals or branched-chain alkyl radicals or branched-chain alkyl radicals, or branched-chain alkyl radicals or branched-chain alkyl radicals or branched-chain alkyl radical
- the ions of the elements of the first to eighth subgroups especially chromium, manganese, iron, cobalt, nickel, copper, zinc and in addition to the second main group, especially calcium and magnesium, of the third and fourth main group, come as metal ions Aluminum, tin and lead are considered.
- the metals can, if appropriate, be present in various valencies to which they are assigned.
- the mixtures of the compounds I, II and III or the compounds I, II and III used simultaneously, together or separately, are distinguished by an excellent action against a broad spectrum of phytopathogenic fungi, in particular from the class of the Ascomycetes, Basidiomycetes, Phycomycetes and Deuteromycetes from. Some of them are systemically effective and can therefore also be used as leaf and soil fungicides.
- the compounds I, II and III can be applied simultaneously, that is jointly or separately, or in succession, the sequence in the case of separate application generally not having any effect on the success of the control measures.
- the compounds I and II are usually in one
- the compounds I and III are usually used in a weight ratio of 10: 1 to 0.01: 1, preferably 5: 1 to 0.05: 1, in particular 1: 1 to 0.05: 1.
- the application rates of the mixtures according to the invention are from 0.01 to 8 kg / ha, preferably 0.1 to 5 kg / ha, in particular 0.2 to 3.0 kg / ha, depending on the type of effect desired.
- the application rates for the compounds I are 0.01 to 2.5 kg / ha, preferably 0.05 to 2.5 kg / ha, in particular 0.1 to 1.0 kg / ha.
- the application rates for the compounds II are accordingly from 0.01 to 10 kg / ha, preferably 0.05 to 5 kg / ha, in particular 0.05 to 2.0 kg / ha.
- the application rates for the compounds III are accordingly from 0.01 to 10 kg / ha, preferably 0.05 to 5 kg / ha, in particular 0.05 to 2.0 kg / ha.
- application rates of mixture of 0.001 to 250 g / kg of seed preferably 0.01 to 100 g / kg, in particular 0.01 to 50 g / kg, are generally used.
- the compounds I, II and III or the mixtures of the compounds I, II and III are applied separately or together by spraying or dusting the seeds, the plants or the soil before or after sowing of the plants or before or after emergence of the plants.
- the fungicidal synergistic mixtures according to the invention or the compounds I, II and III can be used, for example, in the form of directly sprayable solutions, powders and suspensions or in the form of high-strength aqueous, oily or other suspensions, dispersions, emulsions, oil dispersions, pastes, dusts, spreading agents or Granules are processed and applied by spraying, atomizing, dusting, scattering or pouring.
- the form of application depends on the intended use; in any case, it should ensure that the mixture according to the invention is as fine and uniform as possible.
- the formulations are prepared in a manner known per se, e.g. by adding solvents and / or carrier substances.
- Inert additives such as emulsifiers or dispersants are usually added to the formulations.
- the surface-active substances are the alkali metal, alkaline earth metal, ammonium salts of aromatic sulfonic acids, for example lignin, phenol, naphthalene and dibutylnaphthalenesulfonic acid, and of fatty acids, alkyl and alkylarylsulfonates, alkyl, lauryl ether and fatty alcohol sulfates, and salts of sulfated hexa- , Hepta- and octadecanols or fatty alcohol glycol ethers, condensation products of sulfonated naphthalene and its derivatives with form aldehyde, condensation products of naphthalene or naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctyl, octyl or nonylphenol, alkylphenol or tributylphenyl
- Powders, materials for broadcasting and dusts can be prepared by mixing or jointly grinding the compounds I, II and III or the mixture of the compounds I, II and III with a solid carrier.
- Granules e.g. coating, impregnation or homogeneous granules
- a solid carrier e.g., a wax, a wax, or a wax.
- Mineral soils such as silica gel, silicas, silica gels, silicates, talc, kaolin, limestone, lime, chalk, boluses, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground plastics and fertilizers are used as fillers or solid carriers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and vegetable products such as grain flour, tree bark, wood and nutshell flour, cellulose powder or other solid carriers.
- mineral soils such as silica gel, silicas, silica gels, silicates, talc, kaolin, limestone, lime, chalk, boluses, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground plastics and fertilizers are used as fillers or solid carriers such as ammonium sulfate, ammonium phosphate, ammonium
- the formulations generally contain 0.1 to 95% by weight, preferably 0.5 to 90% by weight, of one of the compounds I, II and III or of the mixture of the compounds I, II and III.
- the active ingredients are used in a purity of 90% to 100%, preferably 95% to 100% (according to the N R or HPLC spectrum).
- the compounds I, II and III, the mixtures or the corresponding formulations are used in such a way that the harmful fungi, their habitat or the plants, seeds, soils, areas, materials or spaces to be kept free by them are mixed with a fungicidally effective amount of the mixture or the
- the application can take place before or after infestation by the harmful fungi. Examples of use
- the active ingredients were prepared separately or together as a 10% emulsion in a mixture of 63% by weight cyclohexanone and 27% by weight emulsifier and diluted with water in accordance with the desired concentration.
- Tri tici (wheat mildew)
- Leaves of wheat seedlings ("early gold” variety) were first treated with the aqueous preparation of the active ingredients. After approximately 15 to 24 hours, the plants were dusted with spores of powdery mildew (Erysiphe graminis var. Tritici). The plants treated in this way were then incubated for 7 days at 20-22 ° C. and a relative atmospheric humidity of 75-80%. The extent of fungal development was then determined.
- ⁇ corresponds to the fungal attack of the treated plants in% and ß corresponds to the fungal attack of the untreated (control)
- the infection of the treated plants corresponds to that of the untreated control plants; with an efficiency of 100, the treated plants did not have any
- aqueous active ingredient preparation which was prepared from a stock solution consisting of 10% active ingredient, 63% cyclohexanone and 27% emulsifier, and 24 hours after drying of the spray coating with spores of powdery mildew (Erysiphe graminis forma specialis tritici).
- the test plants were then placed in the greenhouse at temperatures between 20 and 24 ° C and 60 to 90% relative humidity. After 7 days, the extent of mildew development was determined visually in% infestation of the entire leaf area.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SI9830108T SI0986304T1 (en) | 1997-06-04 | 1998-05-20 | Fungicidal mixture |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19723281 | 1997-06-04 | ||
DE19723281 | 1997-06-04 | ||
PCT/EP1998/002946 WO1998054969A1 (de) | 1997-06-04 | 1998-05-20 | Fungizide mischung |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0986304A1 true EP0986304A1 (de) | 2000-03-22 |
EP0986304B1 EP0986304B1 (de) | 2002-07-24 |
Family
ID=7831287
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP98929343A Expired - Lifetime EP0986304B1 (de) | 1997-06-04 | 1998-05-20 | Fungizide mischung |
Country Status (27)
Country | Link |
---|---|
US (1) | US6369090B1 (de) |
EP (1) | EP0986304B1 (de) |
JP (1) | JP4446494B2 (de) |
KR (1) | KR100458241B1 (de) |
CN (1) | CN1292658C (de) |
AR (1) | AR015854A1 (de) |
AT (1) | ATE220855T1 (de) |
AU (1) | AU749368B2 (de) |
BR (1) | BR9809720B1 (de) |
CA (1) | CA2291761C (de) |
CO (1) | CO5031327A1 (de) |
CZ (1) | CZ298787B6 (de) |
DE (1) | DE59804901D1 (de) |
DK (1) | DK0986304T3 (de) |
EA (1) | EA002383B1 (de) |
ES (1) | ES2181237T3 (de) |
HU (1) | HU224639B1 (de) |
IL (1) | IL132911A (de) |
NZ (1) | NZ501240A (de) |
PL (1) | PL189807B1 (de) |
PT (1) | PT986304E (de) |
SI (1) | SI0986304T1 (de) |
SK (1) | SK283266B6 (de) |
TW (1) | TW568751B (de) |
UA (1) | UA68353C2 (de) |
WO (1) | WO1998054969A1 (de) |
ZA (1) | ZA984757B (de) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA72490C2 (uk) * | 1998-12-22 | 2005-03-15 | Басф Акцієнгезелльшафт | Фунгіцидна суміш та спосіб боротьби з фітопатогенними грибами |
KR100311846B1 (ko) * | 1999-07-05 | 2001-10-18 | 우종일 | 신규 아크릴레이트계 살균제 |
ES2282668T3 (es) * | 2002-06-20 | 2007-10-16 | Basf Aktiengesellschaft | Mezclas fungicidas a base de derivados de benzamidoxima de benzofenonas y de un azol. |
DE10248335A1 (de) * | 2002-10-17 | 2004-05-06 | Bayer Ag | Fungizide Wirkstoffkombinationen |
UA85690C2 (ru) * | 2003-11-07 | 2009-02-25 | Басф Акциенгезелльшафт | Смесь для применения в сельском хозяйстве, содержащая стробилурин и модулятор этилена, способ обработки и борьбы с инфекциями в бобовых культурах |
WO2007048534A1 (en) * | 2005-10-26 | 2007-05-03 | Syngenta Participations Ag | Fungicidal compositions |
NZ567996A (en) | 2005-11-10 | 2010-04-30 | Basf Se | Fungicidal mixtures |
PL1947944T3 (pl) * | 2005-11-10 | 2012-09-28 | Basf Se | Zastosowanie piraklostrobiny jako środka zabezpieczającego dla tritikonazolu do zwalczania szkodliwych grzybów |
CA2663436A1 (en) * | 2006-10-04 | 2008-04-10 | Pfizer Products Inc. | Pyrido[4,3-d]pyrimidin-4(3h)-one derivatives as calcium receptor antagonists |
AU2008340152B2 (en) * | 2007-12-21 | 2012-06-07 | Basf Se | Method of increasing the milk and/or meet quantity of silage-fed animals |
JP5365158B2 (ja) * | 2008-11-25 | 2013-12-11 | 住友化学株式会社 | 植物病害防除用組成物及び植物病害の防除方法 |
TWI426568B (zh) * | 2010-03-29 | 2014-02-11 | Sinopower Semiconductor Inc | 半導體功率元件與其製作方法 |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3935113A1 (de) | 1989-10-21 | 1991-04-25 | Basf Ag | Fungizide mischung |
DE4030038A1 (de) | 1990-09-22 | 1992-03-26 | Basf Ag | Ortho-substituierte phenylessigsaeureamide |
DE4139637A1 (de) * | 1991-12-02 | 1993-06-03 | Bayer Ag | Fungizide wirkstoffkombinationen |
DE4309272A1 (de) | 1993-03-23 | 1994-09-29 | Basf Ag | Fungizide Mischung |
DK0645087T3 (da) * | 1993-09-24 | 1996-05-13 | Basf Ag | Fungicide blandinger |
ATE136734T1 (de) * | 1993-09-24 | 1996-05-15 | Basf Ag | Fungizide mischungen |
DE4343176A1 (de) * | 1993-12-17 | 1995-06-22 | Basf Ag | Fungizide Mischung |
EP0737421A4 (de) * | 1993-12-27 | 1998-09-02 | Sumitomo Chemical Co | Bakterizide zusammensetzung |
DE4423613A1 (de) | 1994-07-06 | 1996-01-11 | Basf Ag | 2-[1',2',4'-Triazol-3'yloxymethylen]-anilide, Verfahren zu ihrer Herstellung und ihre Verwendung |
DE4423612A1 (de) | 1994-07-06 | 1996-01-11 | Basf Ag | 2-[(Dihydro)pyrazolyl-3'-oxymethylen]-anilide, Verfahren zu ihrer Herstelung und ihre Verwendung |
AU6122496A (en) * | 1995-06-20 | 1997-01-22 | Pharma-Vinci A/S | A method of preparing an oral preparation provided on the outer side with an enteric coating, as well as an oral preparation obtained by the method |
DE69608806T2 (de) * | 1995-08-18 | 2000-11-02 | Novartis Ag, Basel | Mikrobizide zusammensetzungen |
AU2387297A (en) * | 1996-04-19 | 1997-11-12 | Dr. Wolman Gmbh | Process for treating wood against infection by moulds harmful to wood |
EP0900009B1 (de) | 1996-04-26 | 2002-03-27 | Basf Aktiengesellschaft | Fungizide mischungen |
BR9708873B1 (pt) * | 1996-04-26 | 2009-05-05 | mistura fungicida, e, processo para controlar fungos nocivos. | |
JP2000509054A (ja) * | 1996-04-26 | 2000-07-18 | ビーエーエスエフ アクチェンゲゼルシャフト | 殺菌剤混合物 |
DE19814092A1 (de) * | 1997-04-15 | 1998-10-22 | Stefes Agro Gmbh | Pflanzenschutzmittel |
-
1998
- 1998-05-20 AU AU79139/98A patent/AU749368B2/en not_active Expired
- 1998-05-20 DE DE59804901T patent/DE59804901D1/de not_active Expired - Lifetime
- 1998-05-20 BR BRPI9809720-2A patent/BR9809720B1/pt not_active IP Right Cessation
- 1998-05-20 EA EA199901071A patent/EA002383B1/ru not_active IP Right Cessation
- 1998-05-20 US US09/424,916 patent/US6369090B1/en not_active Expired - Lifetime
- 1998-05-20 NZ NZ501240A patent/NZ501240A/en not_active IP Right Cessation
- 1998-05-20 CN CNB988058103A patent/CN1292658C/zh not_active Expired - Lifetime
- 1998-05-20 SI SI9830108T patent/SI0986304T1/xx unknown
- 1998-05-20 WO PCT/EP1998/002946 patent/WO1998054969A1/de active IP Right Grant
- 1998-05-20 CA CA002291761A patent/CA2291761C/en not_active Expired - Lifetime
- 1998-05-20 ES ES98929343T patent/ES2181237T3/es not_active Expired - Lifetime
- 1998-05-20 CZ CZ0435399A patent/CZ298787B6/cs not_active IP Right Cessation
- 1998-05-20 EP EP98929343A patent/EP0986304B1/de not_active Expired - Lifetime
- 1998-05-20 HU HU0002765A patent/HU224639B1/hu active IP Right Grant
- 1998-05-20 SK SK1634-99A patent/SK283266B6/sk not_active IP Right Cessation
- 1998-05-20 KR KR10-1999-7011336A patent/KR100458241B1/ko not_active IP Right Cessation
- 1998-05-20 AT AT98929343T patent/ATE220855T1/de active
- 1998-05-20 PT PT98929343T patent/PT986304E/pt unknown
- 1998-05-20 PL PL98337191A patent/PL189807B1/pl unknown
- 1998-05-20 UA UA2000010047A patent/UA68353C2/uk unknown
- 1998-05-20 DK DK98929343T patent/DK0986304T3/da active
- 1998-05-20 IL IL13291198A patent/IL132911A/en not_active IP Right Cessation
- 1998-05-20 JP JP50139299A patent/JP4446494B2/ja not_active Expired - Lifetime
- 1998-06-03 TW TW087108722A patent/TW568751B/zh not_active IP Right Cessation
- 1998-06-03 CO CO98031431A patent/CO5031327A1/es unknown
- 1998-06-03 ZA ZA9804757A patent/ZA984757B/xx unknown
- 1998-06-04 AR ARP980102637A patent/AR015854A1/es active IP Right Grant
Non-Patent Citations (1)
Title |
---|
See references of WO9854969A1 * |
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